BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro)

    K Number: K241979 · Decision Aug 22, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    220
    Registration Numbers
    220
    Same Product Code
    1171
    Applicant Total
    2
    Review Days
    48

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    Basic Information

    Device Name
    Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro)
    K Number
    K241979
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.1550
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Beijing Konted Medical Technology Co.,Ltd
    Date Received
    July 5, 2024
    Decision Date
    August 22, 2024
    Product Code
    IYN
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    IYN System, Imaging, Pulsed Doppler, Ultrasonic

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    Other Clearances by Beijing Konted Medical Technology Co.,Ltd

    K Number Device Name
    K231354 Pocket Ultrasound System (C10)